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  • 1
    ISSN: 1573-1421
    Keywords: Rio de la Plata ; La Plata ; Argentina ; Postpampeano ; sedimentary pyrite oxidation ; sulfur cycling ; coastal plain ; sulfur isotopes ; oxygen isotopes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract Groundwater of the coastal plain of the Rio de La Plata, Argentina,contains up to 17 g L-1 SO4 and 37 gL-1 TDS. Some of this SO4 is from paleo-seawater intrusion; however, SO4 : Cl ratios can be〉2 : 1, and most of the SO4 must, therefore, have another source. Three possible sources were investigated: gypsum, organic matter,and iron sulphides. Dissolved SO4 showed δ34S valuesfrom -7 to 0‰, typical values for S from iron sulphides or organicmatter, but distinct from that of seawater (+22‰). To test whetherthe SO4 was derived from oxidation of reduced S, four 4-mcores were taken from marine sediments of the coastal plain. Two were takenfrom higher, drier areas where the highest dissolved SO4values were encountered, and two were taken from lower, wetter areas thathad much lower SO4 concentrations. Pore waterSO4, Cl and alkalinity were determined; solids were analyzedfor SO4, sulphide-S and organic-S. Sulphide-S was the dominant form of reduced S, averaging about0.5% S in the lower interval (2.5–4 m) of the cores. Sulphidewas absent in the upper 2.5 m in both topographically higher and lowerareas. Sulphate was present in the entire unit in the higher, drier areas,but almost absent in lower areas. Organic-S was insignificant. Our model for the origin of dissolved SO4 is: fine-grainedpyrite was oxidized during hotter or drier periods. Some resulting dissolvedSO4 was precipitated as gypsum. Iron from the pyriteprecipitated as FeOOH. Lower, wetter areas formed over time where recharginggroundwater dissolved most of the gypsum. In higher areas with low hydraulicgradients and high net evapotranspiration, SO4 remained asgypsum and in the dissolved phase.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1573-2932
    Keywords: desorption ; ferrihydrite ; modelling ; phosphate ; TEM ; transformation ; wastewater
    Source: Springer Online Journal Archives 1860-2000
    Topics: Energy, Environment Protection, Nuclear Power Engineering
    Notes: Abstract The presence of phosphate retards the transformation of ferrihydrite into crystalline products. Increasing phosphate from 0 to 1 mole % results in an order of magnitude decrease in the rate of transformation of ferrihydrite at pH 12. Levels of phosphate of ∼1 mol % suppress the formation of goethite (α-FeO(OH)) and result in the formation of a product consisting of η-Fe2O3. Higher levels of phosphate result in the ferrihydrite remaining amorphous, even after several hundred hours. Phosphate prevents formation of goethite by hindering the dissolution of ferrihydrite rather than by interfering with nucleation and growth of goethite in solution. The transformation rate of pure ferrihydrite is also strongly inhibited in the presence of dissolved phosphate. This is due to surface complexation. The transformation rate was measured at temperatures of 60 °C and 70 °C. The rate of transformation was found to be described by either (i) a solid-state reaction equation for powdered compacts or (ii) a zero-order reaction controlled by desorption. The transformation of the ferrihydrite matrix was accompanied by the loss of the phosphate trace component. X-ray diffraction indicates that no solid solution involving phosphate substitution into η-Fe2O3 is formed. Transmission electron microphotographs of the original precipitates containing phosphate confirm the presence of the phosphate and demonstrate its involvement in linking together extremely small particles of ferrihydrite.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1573-2932
    Keywords: desorption ; ferrihydrite ; modelling ; phosphate ; TEM ; transformation ; wastewater
    Source: Springer Online Journal Archives 1860-2000
    Topics: Energy, Environment Protection, Nuclear Power Engineering
    Notes: Abstract The presence of phosphate retards the transformation of ferrihydrite into crystalline products. Increasing phosphate from 0 to 1 mole % results in an order of magnitude decrease in the rate of transformation of ferrihydrite at pH 12. Levels of phosphate of ∼1 mol % suppress the formation of goethite (α-FeO(OH)) and result in the formation of a product consisting ofη-Fe2O3. Higher levels of phosphate result in the ferrihydrite remaining amorphous, even after several hundred hours. Phosphate prevents formation of goethite by hindering the dissolution of ferrihydrite rather than by interfering with nucleation and growth of goethite in solution. The transformation rate of pure ferrihydrite is also strongly inhibited in the presence of dissolved phosphate. This is due to surface complexation. The transformation rate was measured at temperatures of 60 °C and 70 °C. The rate of transformation was found to be described by either (i) a solid-state reaction equation for powdered compacts or (ii) a zero-order reaction controlled by desorption. The transformation of the ferrihydrite matrix was accompanied by the loss of the phosphate trace component. X-ray diffraction indicates that no solid solution involving phosphate substitution intoη-Fe2O3 is formed. Transmission electron microphotographs of the original precipitates containing phosphate confirm the presence of the phosphate and demonstrate its involvement in linking together extremely small particles of ferrihydrite.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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